Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Ivette Buendía-Roldan"'
Autor:
Yadira Velasco-Torres, Victor Ruiz López, Oliver Pérez-Bautista, Ivette Buendía-Roldan, Alejandra Ramírez-Venegas, Julia Pérez-Ramos, Ramcés Falfán-Valencia, Carlos Ramos, Martha Montaño
Publikováno v:
BMC Pulmonary Medicine, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Chronic obstructive pulmonary disease (COPD) is characterized by persistent respiratory symptoms and airflow limitation that is due to airway and/or alveolar abnormalities. The main causes of COPD are Gene-environment interactions
Externí odkaz:
https://doaj.org/article/eda09750b7ca45e4bb7d8f7f4a6b849f
Autor:
Oliver Pérez-Bautista, Martha Montaño, Rogelio Pérez-Padilla, Joaquín Zúñiga-Ramos, Mariana Camacho-Priego, Tonatiuh Barrientos-Gutiérrez, Ivette Buendía-Roldan, Yadira Velasco-Torres, Carlos Ramos
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background The main causes of COPD are tobacco smoking (COPD-TS) and biomass smoke exposure (COPD-BS). COPD-TS is known to induce changes in adipokines, incretins, and peptide hormones, frequent biomarkers of inflammation; however, it is unk
Externí odkaz:
https://doaj.org/article/460c4dd9ef4e4856bd7649bbc7f41b4f
Autor:
Marc A. Sala, Yalbi Itzel Balderas-Martínez, Ivette Buendía-Roldan, Hiam Abdala-Valencia, Kiwon Nam, Manu Jain, Sangeeta Bhorade, Ankit Bharat, Paul A. Reyfman, Karen M. Ridge, Annie Pardo, Jacob I. Sznajder, G. R. Scott Budinger, Alexander V. Misharin, Moises Selman
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Idiopathic pulmonary fibrosis (IPF) is characterized by progressive scarring of the lung parenchyma, leading to respiratory failure and death. High resolution computed tomography of the chest is often diagnostic for IPF, but its cost and the
Externí odkaz:
https://doaj.org/article/0f2f4f45c02a430d882d843d62500de3
Autor:
Chintan K. Gandhi, Chixiang Chen, Shaili Amatya, Lili Yang, Chenqi Fu, Shouhao Zhou, Rongling Wu, Ivette Buendía-Roldan, Moisés Selman, Annie Pardo, Joanna Floros
Publikováno v:
Frontiers in Medicine, Vol 7 (2021)
Background: Hypersensitivity pneumonitis (HP) is an interstitial lung disease caused by inhalation of common environmental organic particles. Surfactant proteins (SPs) play a role in innate immunity and surfactant function. We hypothesized that singl
Externí odkaz:
https://doaj.org/article/18b746747606460eb2fce7733159d703
Autor:
Lina Marcela Barranco-Garduño, Ivette Buendía-Roldan, Juan Jose Rodriguez, Rodrigo González-Ramírez, Ariadna N. Cervantes-Nevárez, Juan Carlos Neri-Salvador, Miriam del Carmen Carrasco-Portugal, Gilberto Castañeda-Hernández, Karen Martinez-Espinosa, Moisés Selman, Francisco Javier Flores-Murrieta
Publikováno v:
Heliyon, Vol 6, Iss 10, Pp e05279- (2020)
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal disease characterized by an abnormal activation of lung epithelium and fibroblasts, as well as an excessive accumulation of extracellular matrix. Pirfenidone was introduced as a therapeut
Externí odkaz:
https://doaj.org/article/ef3d41efaf1b44298bdcd6406e562753
Autor:
Ivette Buendía-Roldan, Rosario Fernández-Plata, Abigail Valdes-Bartolo, Mayra Mejia, Luis E. Jaramillo, David Martínez-Briseño, Armando Santiago-Ruiz, Hugo Tapia-Aguilar, Brenda Gómez-Zamora, Annie Pardo, Moises Selman
Publikováno v:
ERJ Open Research, Vol 6, Iss 3 (2020)
Introduction Phenotypic age better represents age-related biological dysregulation than chronological age. Recently, a multisystem-based ageing measure, which integrates chronological age and nine biomarkers, was proposed. Methods Phenotypic age was
Externí odkaz:
https://doaj.org/article/1e5811cdc8f54fe59c39a04c122c9720
Autor:
Laura M. Santiago-Fuentes, Sonia Charleston-Villalobos, Ramón González-Camarena, Andreas Voss, Mayra E. Mejía-Avila, Ivette Buendía-Roldan, Sina Reulecke, Tomás Aljama-Corrales
Publikováno v:
Frontiers in Network Physiology. 2
Idiopathic pulmonary fibrosis (IPF) is a chronic and restrictive disease characterized by fibrosis and inflammatory changes in lung tissue producing a reduction in diffusion capacity and leading to exertional chronic arterial hypoxemia and dyspnea. F
Autor:
Ivette Buendia‐Roldan, Karen Martínez‐Espinosa, Maria‐Jose Aguirre, Hiram Aguilar‐Duran, Alexia Palma‐Lopez, Yadira Palacios, Andy Ruiz, Lucero A. Ramón‐Luing, Ranferi Ocaña‐Guzmán, Gloria Pérez‐Rubio, Ramcés Falfán‐Valencia, Moisés Selman, Leslie Chavez‐Galan
Publikováno v:
Immunity, Inflammation and Disease, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Persistent respiratory symptoms and lung abnormalities post‐COVID‐19 are public health problems. This study evaluated biomarkers to stratify high‐risk patients to the development or persistence of post‐COVID‐19 interstit
Externí odkaz:
https://doaj.org/article/c31221dfb90f4bafa8e953dd73c67f3e
Autor:
María Fernanda López-Bielma, Ramcés Falfán-Valencia, Aurelio Fierro-Piña, Edgar Abarca-Rojano, Elizabeth Córdoba-Lanus, Ingrid Fricke-Galindo, Priscila Romero-Villaseñor, Ivette Buendía-Roldán, Leslie Chávez-Galán, María Esther Jaime-Capetillo, Gloria Pérez-Rubio
Publikováno v:
Heliyon, Vol 10, Iss 8, Pp e29493- (2024)
Introduction: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of Coronavirus Disease 2019 (COVID-19). The disease has a wide range of clinical manifestations, from asymptomatic to severe. Ancestral contribution
Externí odkaz:
https://doaj.org/article/90e202bdb6b544a1aeb6fded628748f6
Autor:
Ana Karem S. Pruneda, José Omar Barreto-Rodríguez, Moises Selman, Fortunato Juárez-Hernández, Ivette Buendía-Roldán
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Since the first case of severe COVID-19, its effect on patients with previous interstitial lung disease (ILD) has been uncertain. We aimed to describe baseline clinical characteristics in ILD patients hospitalized by critical COVI
Externí odkaz:
https://doaj.org/article/a7ac071b2bad4fe08de292478b86f2a8